HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782578Generated: October 30, 2026
Diisopropylethylamine → HCID 68972293, compound
https://huagongshe.com/reaction/1782578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Pyridinecarbonyl chloride, hydrochloride (1:1) | HCID 88438 | — |
| Reactant | HCID 68975066 | HCID 68975066 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68972293 | HCID 68972293 | 39% |
Reaction Steps
A solution of the above nitrile (0.20 g, 0.65 mmol) and nicotinoyl chloride hydrochloride (0.46 g, 2.6 mmol) in THF (6 mL) was then treated with DIPEA (0.56 mL, 3.2 mmol) and stirred at 80° C. for 16 h. The reaction was cooled to room temperature, concentrated under reduced pressure, diluted with CH2Cl2 (10 mL) and washed with brine solution (2×10 mL). The combined organic extracts were then dried (Na2SO4), filtered and concentrated and the crude material purified by flash column chromatography on silica gel (50:1:0.1 CH2Cl2/MeOH/NH4OH) to afford N-[(R)-1-(2-cyano-1-methyl-ethyl)-piperidin-4-yl]-N-(4-difluoromethoxy-phenyl)-nicotinamide as a pale yellow oil (104 mg, 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07498346B2 |
|---|
| Source dataset | uspto-grants-2009_03 |
|---|
| ORD ID | ord-509ba96307904656baf9865e99f729ea |
|---|
| Source note | uspto-grants-2009_03 |
|---|